Source: HPO

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes 		group 0.110 None 1.000 0 0 2011 2011
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C4551915
Disease: Gait Disturbance, CTCAE
Gait Disturbance, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C1145670
Disease: Respiratory Failure
Respiratory Failure 		disease 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C0948163
Disease: Leukoaraiosis
Leukoaraiosis 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C0694550
Disease: Recurrent pneumonia
Recurrent pneumonia 		disease 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C0581354
Disease: Recurrent sinusitis
Recurrent sinusitis 		disease 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C0575081
Disease: Gait abnormality
Gait abnormality 		group 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C0476486
Disease: Generalized enlarged lymph nodes
Generalized enlarged lymph nodes 		disease 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C0349588
Disease: Short stature
Short stature 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C1262477
Disease: Weight decreased
Weight decreased 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C1837066
Disease: Recurrent viral infection
Recurrent viral infection 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C4025790
Disease: Specific learning disability
Specific learning disability 		disease 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C4021850
Disease: Increased sensitivity to ionizing radiation
Increased sensitivity to ionizing radiation 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C4021206
Disease: Chromosomal breakage induced by ionizing radiation
Chromosomal breakage induced by ionizing radiation 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C4012968
Disease: Mild global developmental delay
Mild global developmental delay 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C3714772
Disease: Recurrent fevers
Recurrent fevers 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C3277226
Disease: Restrictive ventilatory defect
Restrictive ventilatory defect 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C1963094
Disease: Dry Skin, CTCAE
Dry Skin, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C1845864
Disease: Poor hand-eye coordination
Poor hand-eye coordination 		phenotype 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy 		disease 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C0270327
Disease: Bedwetting
Bedwetting 		disease 0.100 None 0 0
Entrez Id: 165918
Gene Symbol: RNF168
RNF168 		ring finger protein 168 0.653 0.731 2.1E-13
CUI: C0240059
Disease: Ventricular hemorrhage
Ventricular hemorrhage 		phenotype 0.100 None 0 0